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. 2014 Jan 10;123(10):1604–1614. doi: 10.1182/blood-2013-09-526020

Figure 3.

Figure 3

Endogenous Tregs show stable interactions with host DCs and interfere with the interaction between donor T cells and DCs in the LNs. (A-C) Intravital imaging of donor T cells (labeled with CMTPX) and host DCs in the popliteal LNs of irradiated CD11c-DTR-EGFP mice in the presence (Tcon:Treg ratio of 3:2) or absence of unlabeled Tregs. In the absence of Tregs, unlabeled T cells were injected to provide an identical number of donor cells. (A) The mean velocity of donor T cells in the presence or absence of eTregs from 4 to 24 hours (hr) posttransplant. (B) The time course of the displacement ratio of donor T-cell movement in the presence or absence of eTregs. (C) Contact time between donor T cells and host DCs with or without eTregs at different time points posttransplant. (D-G) Intravital imaging of donor eTregs (labeled with CMTPX) and host DCs in the presence of unlabeled Tcons. (D) Still image from movies of eTreg (red) with DCs (green). (E) Comparison of mean velocity between eTregs and Tcons cells at various time points after transplant. (F) Contact time between eTregs and host DCs, compared with contact time between donor T cells and DCs. (G) Comparison of mean velocity between eTregs and Tcons when they were injected into the same recipient. The bars in all graphs represent median values. Asterisks indicate statistically significant differences between time points (*P < .05) or P value is shown. Data are representative of 2 separate experiments with 1 mouse imaged per condition per experiment.